tert-Butyl isothiocyanate → HCID 22048927, compound

HRID 2087776Notes

Reaction equation

HRID 2087776 reaction equation
[N:1]([C:4]([CH3:7])([CH3:6])[CH3:5])=[C:2]=[S:3].[NH2:8][CH2:9][CH2:10][CH2:11][N:12]1[CH2:17][CH2:16][CH:15]([C:18]2[CH:19]=[C:20]([NH:24][C:25](=[O:29])[CH:26]([CH3:28])[CH3:27])[CH:21]=[CH:22][CH:23]=2)[CH2:14][CH2:13]1>>[C:4]([NH:1][C:2]([NH:8][CH2:9][CH2:10][CH2:11][N:12]1[CH2:17][CH2:16][CH:15]([C:18]2[CH:19]=[C:20]([NH:24][C:25](=[O:29])[CH:26]([CH3:27])[CH3:28])[CH:21]=[CH:22][CH:23]=2)[CH2:14][CH2:13]1)=[S:3])([CH3:7])([CH3:6])[CH3:5]

Participants

3

Reactant 2

HCID 11544tert-Butyl isothiocyanateHCID 16757470N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}2-methylpropanamide

Product 1

HCID 22048927HCID 22048927, compound

Procedure

Prepared by Procedure P and Scheme AB using 2-isothiocyanato-2-methylpropane and N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}-2-methylpropanamide: ESMS m/e: 419.0 (M+H)+.

Workup

  1. customPrepared by Procedure P and Scheme AB

Sources & evidence

ORD record
ord-929a73ab5dfd49ad80b7b1237f880660
Source dataset
uspto-grants-2004_04
Patent number
US06727264B1

Reaction notes

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